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Articles published by Immix Biopharma, Inc.

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Immix Biopharma Announces Major Comprehensive Cancer Center as Lead Site for NXC-201 AL Amyloidosis Clinical Trial
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces “Be Proactive in AL” AL Amyloidosis Awareness Initiative
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Closing of $15 Million Public Offering of Common Stock
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Awarded European Union Orphan Drug Designation for NXC-201 in AL Amyloidosis
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Pricing of $15 Million Public Offering of Common Stock
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Proposed Public Offering of Common Stock
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Statement On January 2024 FDA Labeling Change Notification For Approved CAR-T Products
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Dr. Vaishali Sanchorawala, AL Amyloidosis Thought Leader, Director of the Amyloidosis Center at Boston University and Boston Medical Center, Joins Scientific Advisory Board
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Dr. Marko Radic, Autoimmune CAR-T Pioneer and Associate Professor at the University of Tennessee Health Science Center, Joins Scientific Advisory Board
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces 100% Overall Response Rate (n=10); 23.7 months Best Response Duration (ongoing) for CAR-T NXC-201 in Relapsed/Refractory AL Amyloidosis Patients at ASH 2023
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma to Present at the 2023 JMP Securities Hematology and Oncology Summit
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma to Host KOL Event to Discuss its BCMA-Targeted CAR-T Cell Therapy Candidate NXC-201 for Relapsed/Refractory AL Amyloidosis
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces FDA Approval of IND Application for CAR-T NXC-201, Enabling U.S. Patient Dosing
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Presents NXC-201 Data at 65th American Society of Hematology (ASH) Annual Meeting in 9 Relapsed/Refractory AL Amyloidosis Patients
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Presents NXC-201 Data at 65th American Society of Hematology (ASH) Annual Meeting in 63 Relapsed/Refractory Multiple Myeloma Patients
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Subsidiary Nexcella Announces Dr. Michaela Liedtke, Stanford Medicine Cancer Center Hematology Program Lead and Co-Director Stanford Amyloid Center, Joins Scientific Advisory Board
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Completes 3rd NXC-201 Engineering Batch at its U.S. CAR-T Manufacturing Site
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Complete Response in 9th Relapsed/Refractory AL Amyloidosis Patient in NXC-201 Clinical Trial at IMS 20th Annual Meeting
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces 72-Patient NXC-201 Clinical Data at the IMS 20th Annual Meeting, 95% Overall Response Rate in Multiple Myeloma
From Immix Biopharma, Inc.
Via GlobeNewswire
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U.S. Food and Drug Administration Approves Orphan Drug Designation for Immix Biopharma NXC-201 as a Treatment for Amyloid Light Chain (AL) Amyloidosis
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Subsidiary Nexcella Completes 2nd NXC-201 Engineering Batch at its U.S. CAR-T Manufacturing Site
From Immix Biopharma, Inc.
Via GlobeNewswire
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Nexcella, Immix Biopharma Subsidiary, to Present at the Bank of America 2023 Healthcare Trailblazers Private Company Conference
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Dr. Suzanne Lentzsch, Director of the Multiple Myeloma and Amyloidosis Program at the College of Physicians and Surgeons of Columbia University and at New York Presbyterian Hospital in New York, Joins Scientific Advisory Board
From Immix Biopharma, Inc.
Via GlobeNewswire
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U.S. Food and Drug Administration Approves Orphan Drug Designation for Immix Biopharma NXC-201 as a Treatment for Multiple Myeloma
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Dr. Heather Landau, Memorial Sloan Kettering Cancer Center Amyloidosis Program Director, Joins Nexcella Scientific Advisory Board
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Announces Additional NXC-201 AL Amyloidosis Clinical Data Accepted for Oral Presentation at the 20th International Myeloma Society Annual Meeting (September 27-30, Athens Greece)
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Subsidiary Nexcella Announces NXC-201 Multiple Myeloma Clinical Data Abstract Accepted for Presentation at the 20th International Myeloma Society Annual Meeting
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Reports 2nd Positive Interim Clinical Trial Data Readout in Relapsed/Refractory Metastatic Colorectal Cancer in Ongoing Phase 1b/2a IMX-110 IMMINENT-01 Clinical Trial
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Subsidiary Nexcella Completes Initial NXC-201 Engineering Batch at its U.S. CAR-T Manufacturing Site
From Immix Biopharma, Inc.
Via GlobeNewswire
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Immix Biopharma Subsidiary Nexcella Completes Pre-IND Meeting with FDA on NXC-201 US Clinical Trial
From Immix Biopharma, Inc.
Via GlobeNewswire
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